نتایج جستجو برای: family history fh

تعداد نتایج: 739379  

2016
Halvor Øygarden Annette Fromm Kristin Modalsli Sand Christopher Elnan Kvistad Geir Egil Eide Lars Thomassen Halvor Naess Ulrike Waje-Andreassen

BACKGROUND AND PURPOSE Positive family history (FH+) of cardiovascular disease (CVD) is a risk factor for own CVD. We aimed to analyze the effect of different types of FH (stroke, coronary heart disease (CHD), peripheral artery disease (PAD) on carotid intima-media thickness (cIMT) in young and middle-aged ischemic stroke patients. METHODS First-degree FH of CVD was assessed in ischemic strok...

2015
Omer A. Raheem Seth A. Cohen J. Kellogg Parsons Kerrin L. Palazzi Christopher J. Kane

We investigated whether a family history of lethal prostate cancer (PCa) was associated with high-risk disease or biochemical recurrence in patients undergoing radical prostatectomy. A cohort of radical prostatectomy patients was stratified into men with no family history of PCa (NFH); a first-degree relative with PCa (FH); and those with a first-degree relative who had died of PCa (FHD). Demog...

2015
QING LI LUAN WANG LIN XIAO ZHONGCHAO WANG FANG WANG XIAOLONG YU SHENGLI YAN YANGANG WANG

Intensive insulin treatment is known to improve β-cell function in the majority of patients with newly diagnosed type 2 diabetes mellitus (T2DM), and family history (FH) is known to be an important independent risk factor for T2DM. Thus, the aim of the present study was to investigate the difference in first-phase insulin secretion and the effect of intensive insulin therapy on the improvement ...

Journal: :Thrombosis and haemostasis 2015
Bengt Zöller Xinjun Li Henrik Ohlsson Jianguang Ji Jan Sundquist Kristina Sundquist

Familial clustering of venous thromboembolism (VTE) was described as far back as 1905 by Briggs. Although Egeberg discovered inherited deficiency of antithrombin in 1965, it was not until Dahlbäck discovered resistance to activated protein C in 1993 that it became clear that genetic factors are common risk factors of VTE. Several genes have been linked to familial aggregation of VTE and genome-...

Journal: :Cancer research 2010
Judy Mouchawar Christopher Korch Tim Byers Todd M Pitts Efang Li Margaret R E McCredie Graham G Giles John L Hopper Melissa C Southey

Although germline TP53 mutations have been identified in women with breast cancer from families meeting Li-Fraumeni criteria, their contribution to breast cancer per se is not well known, but is thought to be minimal. We aimed to determine the prevalence of germline TP53 mutations in subgroups of early-onset breast cancer. Germline TP53 mutation status was assessed by DNA sequencing, screening ...

Journal: :Circulation. Cardiovascular genetics 2011
Amitava Banerjee Chris C S Lim Louise E Silver Sarah J V Welch Adrian P Banning Peter M Rothwell

BACKGROUND Stroke in female first-degree relatives (FDRs) is a powerful risk factor for ischemic stroke in women, but its association with acute coronary syndromes (ACS) is unknown. Family history (FH) of stroke is omitted from existing myocardial infarction risk prediction tools, which perform less well in women than in men. Our objective was to study the sex-of-parent and sex-of-proband inter...

Journal: :Hypertension 1984
M L Tuck C Gross M H Maxwell A S Brickman G Krasnoshtein D Mayes

Alterations in red blood cell (RBC) Na+,K+ pump and in Na+,K+ cotransport (CoT) have been described in essential hypertension (EH). We examined pump and CoT in 50 normotensive (NT) subjects and 58 EH subjects subdivided by race and family history of hypertension (+ FH). RBCs were preloaded with Na+ to obtain intracellular levels of 25 mM/liter cells by using the p-chloromercuribenzene sulfonic ...

2008
Guofan Xu Donald G. Mclaren Michele L. Ries Michele E. Fitzgerald Barbara B. Bendlin Howard A. Rowley Mark A. Sager Craig Atwood Sanjay Asthana Sterling C. Johnson

First-degree family history (FH) of sporadic Alzheimer’s disease and the apolipoprotein E e4 allele (APOE4) are risk factors for Alzheimer’s disease that may affect brain function prior to onset of clinical symptoms. In this functional MRI (fMRI) study, we used an episodic recognition task that required discrimination of previously viewed (PV) and novel (NV) faces to examine differences in bloo...

2015
James C. Barton J. Clayborn Barton

We performed a retrospective study of autoimmune conditions (ACs) in 235 hemochromatosis probands at diagnosis by analyzing age, sex, ACs, history of first-degree family members with ACs (FH), diabetes, heavy ethanol consumption, elevated serum ALT/AST, nonalcoholic fatty liver disease, viral hepatitis, cirrhosis, iron removed to achieve iron depletion (QFe), and positivity for human leukocyte ...

Journal: :iranian journal of diabetes and obesity 0
elaheh asadi department of genetics, faculty of medicine, shahid sadoughi university of medical sciences, yazd, iran. ehsan farashahi yazd department of genetics, faculty of medicine, shahid sadoughi university of medical sciences, yazd, iran.research and clinical centre for infertility, shahid sadoughi university of medical sciences, yazd, iran. mohammad hassan sheikhha department of genetics, faculty of medicine, shahid sadoughi university of medical sciences, yazd, iran.research and clinical centre for infertility, shahid sadoughi university of medical sciences, yazd, iran. nasrin ghasemi department of genetics, faculty of medicine, shahid sadoughi university of medical sciences, yazd, iran. razieh zarifian yeganeh department of medical genetics, tehran university of medical sciences, tehran, iran.

familial hypercholesterolemia (fh) is an inherited common autosomal mendelian disorder of lipoprotein metabolism with a population prevalence of 1 in 500. fh is characterized by severely elevated levels of low-density lipoprotein cholesterol (ldl-c), which result in surplus deposition of cholesterol in tissues. this condition leads to premature at hero sclerosis and early-onset of coronary hear...

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